Germline mutations in succinate dehydrogenase B (SDHB) predispose to hereditary paraganglioma (PGL) syndrome type 4. The risk of developing PGL or pheochromocytoma (PHEO) in SDHB mutation carriers is subject of recent debate. In the present nationwide cohort study of SDHB mutation carriers identified by the clinical genetics centers of the Netherlands, we have calculated the penetrance of SDHB associated tumors using a novel maximum likelihood estimator. This estimator addresses ascertainment bias and missing data on pedigree size and structure. A total of 195 SDHB mutation carriers were included, carrying 27 different SDHB mutations. The 2 most prevalent SDHB mutations were Dutch founder mutations: a deletion in exon 3 (31% of mutation carriers) and the c.423+1G>A mutation (24% of mutation carriers). One hundred and twelve carriers (57%) displayed no physical, radiological or biochemical evidence of PGL or PHEO. Fifty-four patients had a head and neck PGL (28%), 4 patients had a PHEO (2%), 26 patients an extra-adrenal PGL (13%). The overall penetrance of SDHB mutations is estimated to be 21% at age 50 and 42% at age 70 when adequately corrected for ascertainment. These estimates are lower than previously reported penetrance estimates of SDHB-linked cohorts. Similar disease risks are found for different SDHB germline mutations as well as for male and female SDHB mutation carriers.

Additional Metadata
Keywords Paraganglioma, Penetrance, Pheochromocytoma, SDHB
Persistent URL dx.doi.org/10.1111/cge.13055, hdl.handle.net/1765/101891
Journal Clinical Genetics: an international journal of genetics and molecular medicine
Citation
Rijken, J.A. (J. A.), Niemeijer, N.D, Jonker, M.A. (M. A.), Eijkelenkamp, K. (K.), Jansen, J.C, Van Berkel, A, … Hensen, E.F. (2017). The penetrance of paraganglioma and pheochromocytoma in SDHB germline mutation carriers. Clinical Genetics: an international journal of genetics and molecular medicine. doi:10.1111/cge.13055